Taiwan FDA registration 276e2a17cd0800ebd5138f3661978c58
“STORZ MEDICAL” Modulith SLX-F2 Lithotripter
TW: “斯拓茲”體外震波碎石機
Taiwan·Risk Class 2·MD·Storz Medical AG·Registered Dec 20, 2022 – Dec 20, 2027ActiveRegistration details
- Analysis ID
- 276e2a17cd0800ebd5138f3661978c58
- License Form
- Ministry of Health Medical Device Import No. 036140
- Customs Code
- DHA05603614004
Company information
- Manufacturer
- Storz Medical AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- KINDMED CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H5990 Extracorporeal shock wave lithotripsy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 20, 2022
- Expiry Date
- Dec 20, 2027
About this record
Access comprehensive regulatory information for “STORZ MEDICAL” Modulith SLX-F2 Lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 276e2a17cd0800ebd5138f3661978c58 and manufactured by Storz Medical AG. The authorized representative in Taiwan is KINDMED CORPORATION.
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